This EO sterilization training Webinar will discuss how to modify EO sterilization process for complicated medical products which are sensitive to moisture, temperature, vacuum changes.
Why Should You Attend:
Medical products have become more complicated with many containing computer chips, batteries, antibiotics, or other items/materials that make sterilization a significant challenge. These products that present difficult challenges to the EO sterilization process may include those products that have sensitivity to temperature, have moisture limitations, are sensitive to vacuum changes (either level or rate), retain EO, have batteries, or a combination of these factors. Developing a sterilization process presents a challenge but in virtually all cases a process can be developed that meets the requirement to have a sterile functional product.
Areas Covered in the Seminar :

• How to limit moisture exposure.
• Running a low temperature process.
• How to address vacuum sensitivity.
• Parameter inter-relationships.
• How to reduce EO residuals.
• Testing outside of the sterilization facility.
• Considerations for validation and routine processing.

Note: Use this Promo Code(102165) to avail Discount of 10% on LIVE Purchase.

This EO sterilization training Webinar will discuss the important parameters to measure for the sterility assurance level and actions to take if they are not compliant to the process specification.
Why Should You Attend: 
Ethylene oxide (EO) sterilization is the most complicated of the industrial sterilization methods. Many anomalies occur during qualification or routine processing and may come in the form of sterilization cycle parameter that is not achieved or a positive biological indicator. Not knowing how to respond to these situations can result in a response that results in the release of product that might not meet the required sterility assurance level (SAL) or the needless re-sterilization of product. Regulatory action can result from the prior while additional expense to the company can result from the latter. But not every parameter in the EO sterilization process in critical for the determination of the SAL.
 
Areas Covered in the Seminar:

• What is a cycle anomaly.
• What cycle specifications are critical for sterilization.
• What cycle specifications are critical for product residuals.
• Actions to be taken for critical deviations/anomalies.
• Actions to be taken for non-critical deviations/anomalies.
• What testing can be performed to justify product release.
• Developing a specification to address actions.
• How to document your rationale.

Note: Use this Promo Code(101460) to avail Discount of 10% on LIVE Purchase.